Canonical Allele Identifier: CA2067768474
Gene: P2RX7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121132976G= , CM000674.2:g.121132976G= GRCh38
NC_000012.11:g.121570779G= , CM000674.1:g.121570779G= GRCh37
NC_000012.10:g.120055162G= NCBI36
NG_011471.2:g.5102G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328963.10:c.6G= MANE Select ENSP00000330696.6:p.Pro2=
ENST00000261826.10:c.6G= ENSP00000261826.6:p.Pro2=
ENST00000328963.9:c.6G= ENSP00000330696.6:p.Pro2=
ENST00000535250.5:c.6G= ENSP00000442572.2:p.Pro2=
ENST00000535600.2:c.6G= ENSP00000442470.1:p.Pro2=
ENST00000535928.5:c.6G= ENSP00000439961.1:p.Pro2=
ENST00000537312.5:c.6G= ENSP00000438586.1:p.Pro2=
ENST00000538011.5:c.6G= ENSP00000439247.1:p.Pro2=
ENST00000539606.5:c.6G= ENSP00000445325.1:p.Pro2=
ENST00000539695.5:n.75G=
ENST00000541022.5:c.6G= ENSP00000441230.1:p.Pro2=
ENST00000541564.5:c.6G= ENSP00000443640.1:p.Pro2=
ENST00000541716.5:c.6G= ENSP00000437729.1:p.Pro2=
ENST00000545434.5:c.6G= ENSP00000445564.1:p.Pro2=
NM_002562.5:c.6G= NP_002553.3:p.Pro2=
NR_033948.1:n.149G=
NR_033949.1:n.149G=
NR_033950.1:n.149G=
NR_033951.1:n.149G=
NR_033952.1:n.149G=
NR_033953.1:n.158G=
NR_033954.1:n.149G=
NR_033955.1:n.149G=
NR_033956.1:n.149G=
XM_011538418.1:c.6G= XP_011536720.1:p.Pro2=
XM_011538419.1:c.-138G= XP_011536721.1:n.-138G=
XM_011538419.3:c.-138G= XP_011536721.1:n.-138G=
XM_017019364.2:c.-508G= XP_016874853.1:n.-508G=
XM_017019365.2:c.-339G= XP_016874854.1:n.-339G=
XM_017019366.2:c.-675G= XP_016874855.1:n.-675G=
XM_017019367.2:c.-506G= XP_016874856.1:n.-506G=
XR_001749352.2:n.187-6135C=
XR_001749354.2:n.187-6135C=
NM_002562.6:c.6G= MANE Select NP_002553.3:p.Pro2=
NR_033948.2:n.101G=
NR_033949.2:n.101G=
NR_033950.2:n.101G=
NR_033951.2:n.101G=
NR_033952.2:n.101G=
NR_033953.2:n.101G=
NR_033954.2:n.101G=
NR_033955.2:n.101G=
NR_033956.2:n.101G=